Council for Rare Diseases (CRD)

The Council for Rare Diseases (CRD) is a professional organization that brings together experts, researchers, and healthcare providers focused on understanding and improving care for rare diseases—conditions that affect a small percentage of the population. Its mission is to promote research, raise awareness, and develop guidelines to ensure patients with rare diseases receive accurate diagnosis, effective treatment, and specialized support. By fostering collaboration among specialists and stakeholders, the CRD aims to advance knowledge and resources to improve quality of life for those affected by these uncommon conditions.